Canonical Allele Identifier: PA2830222857
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Leu21057Met
CA183587
NM_133432.3:c.63169T>A